Canonical Allele Identifier: CA236608869
Gene: WNT1 HGNC NCBI

Linked Data

dbSNP Id: rs183334037
gnomAD v2: 12-49375538-C-A
gnomAD v3: 12-48981755-C-A
gnomAD v4: 12-48981755-C-A
MyVariant Identifiers: chr12:g.49375538C>A (hg19) chr12:g.48981755C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.48981755C>A , CM000674.2:g.48981755C>A GRCh38
NC_000012.11:g.49375538C>A , CM000674.1:g.49375538C>A GRCh37
NC_000012.10:g.47661805C>A NCBI36
NG_033141.1:g.8303C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000293549.4:c.*115C>A MANE Select ENSP00000293549.3:n.*115C>A
NM_005430.3:c.*115C>A NP_005421.1:n.*115C>A
NM_005430.4:c.*115C>A MANE Select NP_005421.1:n.*115C>A
Search 100 bp 5'
Search 100 bp 3'